FILT-R-ALL BACTERIAL/VIRAL FILTER— 510(k) K900990

Name: FDA 510(k) clearance K900990
Creator: U.S. Food and Drug Administration
Published: 1990-04-19

Substantially Equivalent

Inhalation Plastics

FDA 510(k) clearance K900990 for FILT-R-ALL BACTERIAL/VIRAL FILTER, Substantially Equivalent on 1990-04-19. Applicant: Inhalation Plastics. Device class: 2.

Clearance details

Applicant: Inhalation Plastics
Product code: Code CAH
Device class: Class 2
Regulation: 21 CFR 868.5260
Advisory panel: Anesthesiology
Date received: 1990-03-02
Decision date: 1990-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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K222917 — Breathing circuit bacterial/viral filter2024-02-15
K230483 — Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)2023-09-16

More clearances from Inhalation Plastics

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K945565 — SPIRO-FLEX1995-01-13
K914686 — THERMO-FLOW SET1992-04-15
K901315 — AEROMIST II NEBULIZER1990-09-10
K900594 — ANESTHESIA BREATHING CIRCUIT1990-03-15
K896832 — FILT-R-ALL BACTERIAL FILTER1990-01-22

Adverse events under product code CAH

product code CAH

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.